2010

Colson, Natalie, Fernandez, Francesca, & (2010) Genetics of menstrual migraine : the molecular evidence. Current Pain and Headache Reports, 14(5), pp. 389-395. (https://eprints.qut.edu.au/62631/)

Formicola, Daniela, Aloia, Andrea, Sampaolo, Simone, Farina, Olimpia, Diodato, Daria, , Gianfrancesco, Fernando, Di Iorio, Giuseppe, & Esposito, Teresa (2010) Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. BMC Medical Genetics, 11(1), p. 103. (https://eprints.qut.edu.au/62590/)

Gabrovska, Plamena N., , , & (2010) Gene expression profiling in human breast cancer – toward personalised therapeutics? Open Breast Cancer Journal, 2, pp. 46-59. (https://eprints.qut.edu.au/63635/)

Green, Michael R., Jardine, Paul, Wood, Peter, Wellwood, Jeremy, , Marlton, Paula, & (2010) A new method to detect loss of heterozygosity using cohort heterozygosity comparisons. BMC Cancer, 10(1), p. 195. (https://eprints.qut.edu.au/62587/)

Lafrenière, Ronald G, Cader, M Zameel, Poulin, Jean-François, Andres-Enguix, Isabelle, Simoneau, Maryse, Gupta, Namrata, Boisvert, Karine, Lafrenière, François, McLaughlan, Shannon, Dubé, Marie-Pierre, Marcinkiewicz, Martin M, Ramagopalan, Sreeram, Ansorge, Olaf, Brais, Bernard, Sequeiros, Jorge, Pereira-Monteiro, Jose Maria, , Tucker, Stephen J., Ebers, George, & Rouleau, Guy A. (2010) A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. Nature Medicine, 16(10), pp. 1157-1160. (https://eprints.qut.edu.au/62586/)

Liu, Annie, , Colson, Natalie J., Quinlan, Sharon, Cox, Hannah, Peterson, Madelyn, Tiang, Thomas, , , & (2010) Analysis of the MTHFR C677T variant with migraine phenotypes. BMC Research Notes, 3(1), p. 213. (https://eprints.qut.edu.au/62589/)

Szvetko, Attila L., Jones, Ashleigh, Mackenzie, Jason, Tajouri, Lotti, Csurhes, Peter A., Greer, Judith M., Pender, Michael P., & (2010) Investigation of the [−/A]<SUB>8</SUB> and C1236T genetic variations within the human toll-like receptor 3 gene for association with multiple sclerosis. Neurological Research, 32(4), pp. 438-441. (https://eprints.qut.edu.au/62632/)